ENST00000642496.1:c.3986G>A
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ENST00000644397.2:c.5127G>A
MANE Select
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ENSP00000495195.1:p.Glu1709=
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ENST00000373965.6:c.4938G>A
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ENSP00000363076.3:p.Glu1646=
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ENST00000414778.5:c.4935G>A
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ENSP00000410304.2:p.Glu1645=
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ENST00000495484.5:c.1155G>A
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ENSP00000480780.1:p.Glu385=
|
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ENST00000614895.4:c.4950G>A
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ENSP00000478512.1:p.Glu1650=
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ENST00000616114.4:c.4932G>A
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ENSP00000483745.1:p.Glu1644=
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ENST00000618301.4:c.1287G>A
|
ENSP00000482780.1:p.Glu429=
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ENST00000621708.4:c.4953G>A
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ENSP00000484454.1:p.Glu1651=
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NM_001142771.1:c.4953G>A
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NP_001136243.1:p.Glu1651=
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|
NM_001142772.1:c.4938G>A
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NP_001136244.1:p.Glu1646=
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|
NM_001354420.1:c.4932G>A
|
NP_001341349.1:p.Glu1644=
|
|
NM_001354429.1:c.5061G>A
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NP_001341358.1:p.Glu1687=
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XR_001747192.2:n.11419G>A
|
|
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XR_001747193.2:n.11410G>A
|
|
|
NM_001142771.2:c.4953G>A
|
NP_001136243.1:p.Glu1651=
|
|
NM_001142772.2:c.4938G>A
|
NP_001136244.1:p.Glu1646=
|
|
NM_001354420.2:c.4932G>A
|
NP_001341349.1:p.Glu1644=
|
|
NM_001354429.2:c.5061G>A
|
NP_001341358.1:p.Glu1687=
|
|
NM_001384140.1:c.5127G>A
MANE Select
|
NP_001371069.1:p.Glu1709=
|
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